[Recalled] Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10. 2. Clavicle Plate; Article Numbers: 2112
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10. 2. Clavicle Plate; Article Numbers: 21121-6, 21121-8. 3. Clavicle Plate, 3.5mm; Article Numbers: 21122-10, |
|---|---|
| Brand / manufacturer | I.T.S. GmbH |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1593-2026 |
| Country of notice | Austria |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 January 2026 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
This Class II recall concerns device products distributed in Austria and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from I.T.S. GmbH
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.